Literature DB >> 11880427

Application of a 5' nuclease assay for detection of Lawsonia intracellularis in fecal samples from pigs.

R H Lindecrona1, T K Jensen, P H Andersen, K Møller.   

Abstract

A 5' nuclease assay was developed to detect Lawsonia intracellularis in porcine fecal samples. The specific probe and primers were chosen by using the 16S ribosomal DNA gene as a target. The 5' nuclease assay was used with a total of 204 clinical samples, and the results were compared to those of immunohistochemistry (IM) on ileal sections of the same animals. There was 91% agreement between the results of IM and the 5' nuclease assay. In the 5' nuclease assay, 111 (54%) of the pigs tested positive for L. intracellularis infection, with a mean cycle threshold (Ct) value of 27.2, whereas 98 (48%) of the pigs tested positive by IM. On average, the Ct and DeltaRn values for the positive samples were 27.2 (standard deviation [SD], 3.7) and 1.6 (SD, 0.7), respectively. A Ct value of 27.2 corresponds to a fecal excretion of approximately 10(7) L. intracellularis cells per g of feces. Furthermore, a total of 40 fecal samples derived from a herd known to be free from infection with L. intracellularis all tested negative, with a Ct value of 40. By using a Ct value of 36 as the cutoff limit, the detection limit of the assay was 1 L. intracellularis cell per PCR tube. In conclusion, the 5' nuclease assay that has been developed represents an applicable fast method for detection of L. intracellularis in fecal samples, with a sensitivity and specificity comparable to those of IM.

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Year:  2002        PMID: 11880427      PMCID: PMC120237          DOI: 10.1128/JCM.40.3.984-987.2002

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  24 in total

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Authors:  G H Lawson; C J Gebhart
Journal:  J Comp Pathol       Date:  2000 Feb-Apr       Impact factor: 1.311

2.  Evaluation of antemortem polymerase chain reaction and serologic methods for detection of Lawsonia intracellularis-exposed pigs.

Authors:  J P Knittel; D M Jordan; K J Schwartz; B H Janke; M B Roof; S McOrist; D L Harris
Journal:  Am J Vet Res       Date:  1998-06       Impact factor: 1.156

3.  Detection of Lawsonia intracellularis in the tonsils of pigs with proliferative enteropathy.

Authors:  T K Jensen; K Møller; R Lindecrona; S E Jorsal
Journal:  Res Vet Sci       Date:  2000-02       Impact factor: 2.534

4.  Monoclonal antibodies to intracellular campylobacter-like organisms of the porcine proliferative enteropathies.

Authors:  S McOrist; R Boid; G H Lawson; I McConnell
Journal:  Vet Rec       Date:  1987-10-31       Impact factor: 2.695

5.  Intracellular bacteria of porcine proliferative enteropathy: cultivation and maintenance in vitro.

Authors:  G H Lawson; S McOrist; S Jasni; R A Mackie
Journal:  J Clin Microbiol       Date:  1993-05       Impact factor: 5.948

6.  Evaluation of 5' nuclease assay for detection of Actinobacillus pleuropneumoniae.

Authors:  O Angen; J Jensen; D T Lavritsen
Journal:  J Clin Microbiol       Date:  2001-01       Impact factor: 5.948

7.  Improved diagnosis of porcine proliferative enteropathy caused by Lawsonia intracellularis using polymerase chain reaction-enzyme-linked oligosorbent assay (PCR-ELOSA).

Authors:  P Zhang; C J Gebhart; D Burden; G E Duhamel
Journal:  Mol Cell Probes       Date:  2000-04       Impact factor: 2.365

8.  Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase.

Authors:  P M Holland; R D Abramson; R Watson; D H Gelfand
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-15       Impact factor: 11.205

9.  Detection of Lawsonia intracellularis, Serpulina hyodysenteriae, weakly beta-haemolytic intestinal spirochaetes, Salmonella enterica, and haemolytic Escherichia coli from swine herds with and without diarrhoea among growing pigs.

Authors:  K Møller; T K Jensen; S E Jorsal; T D Leser; B Carstensen
Journal:  Vet Microbiol       Date:  1998-04-30       Impact factor: 3.293

10.  Detection of Lawsonia intracellularis in swine using polymerase chain reaction methodology.

Authors:  D M Jordan; J P Knittel; M B Roof; K Schwartz; D Larson; L J Hoffman
Journal:  J Vet Diagn Invest       Date:  1999-01       Impact factor: 1.279

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  5 in total

1.  Application of a pig ligated intestinal loop model for early Lawsonia intracellularis infection.

Authors:  Torsten S Boutrup; Kirsten Schauser; Jørgen S Agerholm; Tim K Jensen
Journal:  Acta Vet Scand       Date:  2010-02-24       Impact factor: 1.695

2.  Development of a high-throughput real-time PCR system for detection of enzootic pathogens in pigs.

Authors:  Nicole B Goecke; Charlotte K Hjulsager; Jesper S Krog; Kerstin Skovgaard; Lars E Larsen
Journal:  J Vet Diagn Invest       Date:  2019-11-21       Impact factor: 1.279

3.  Human inflammatory bowel disease does not associate with Lawsonia intracellularis infection.

Authors:  Christoph W Michalski; Fabio Francesco Di Mola; Klaus Kümmel; Michael Wendt; Jörg S Köninger; Thomas Giese; Nathalia A Giese; Helmut Friess
Journal:  BMC Microbiol       Date:  2006-09-19       Impact factor: 3.605

4.  Bacillus pumilus probiotic feed supplementation mitigates Lawsonia intracellularis shedding and lesions.

Authors:  Tanja Opriessnig; Anbu K Karuppannan; Dana Beckler; Tahar Ait-Ali; Ana Cubas-Atienzar; Patrick G Halbur
Journal:  Vet Res       Date:  2019-10-22       Impact factor: 3.683

5.  Down-regulation of mechanisms involved in cell transport and maintenance of mucosal integrity in pigs infected with Lawsonia intracellularis.

Authors:  Sionagh H Smith; Alison D Wilson; Imke Van Ettinger; Neil MacIntyre; Alan L Archibald; Tahar Ait-Ali
Journal:  Vet Res       Date:  2014-05-20       Impact factor: 3.683

  5 in total

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